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Rapp-Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi).
Birth Defects Orig Artic Ser. 1988; 24(2):149-68.BD

Abstract

We have reported on six personally examined patients with Rapp Hodgkin syndrome and four additional family members with documentation suggesting strongly that they also were affected with the disorder. Clinical manifestations observed in our patients include cleft lip/palate/uvula, ectodermal dysplasia, and hypospadias in males. The ectodermal dysplasia manifests through uncombable, sparse, wiry hair; alopecia in adulthood; hypodontia; hypohidrosis; and dysplastic nails. In addition, ptosis, atretric ear canals, and dysplastic eustachian orifices are suggested as other manifestations of the disorder.

Authors+Show Affiliations

College of Dental Medicine, Department of Diagnostic Science, Medical University of South Carolina, Charleston 29425.No affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

3179424

Citation

Salinas, C F., and G M. Montes. "Rapp-Hodgkin Syndrome: Observations On Ten Cases and Characteristic Hair Changes (pili Canaliculi)." Birth Defects Original Article Series, vol. 24, no. 2, 1988, pp. 149-68.
Salinas CF, Montes GM. Rapp-Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi). Birth Defects Orig Artic Ser. 1988;24(2):149-68.
Salinas, C. F., & Montes, G. M. (1988). Rapp-Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi). Birth Defects Original Article Series, 24(2), 149-68.
Salinas CF, Montes GM. Rapp-Hodgkin Syndrome: Observations On Ten Cases and Characteristic Hair Changes (pili Canaliculi). Birth Defects Orig Artic Ser. 1988;24(2):149-68. PubMed PMID: 3179424.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Rapp-Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi). AU - Salinas,C F, AU - Montes,G M, PY - 1988/1/1/pubmed PY - 1988/1/1/medline PY - 1988/1/1/entrez SP - 149 EP - 68 JF - Birth defects original article series JO - Birth Defects Orig Artic Ser VL - 24 IS - 2 N2 - We have reported on six personally examined patients with Rapp Hodgkin syndrome and four additional family members with documentation suggesting strongly that they also were affected with the disorder. Clinical manifestations observed in our patients include cleft lip/palate/uvula, ectodermal dysplasia, and hypospadias in males. The ectodermal dysplasia manifests through uncombable, sparse, wiry hair; alopecia in adulthood; hypodontia; hypohidrosis; and dysplastic nails. In addition, ptosis, atretric ear canals, and dysplastic eustachian orifices are suggested as other manifestations of the disorder. SN - 0547-6844 UR - https://wwww.unboundmedicine.com/medline/citation/3179424/Rapp_Hodgkin_syndrome:_observations_on_ten_cases_and_characteristic_hair_changes__pili_canaliculi__ L2 - https://www.diseaseinfosearch.org/result/6153 DB - PRIME DP - Unbound Medicine ER -